Canonical Allele Identifier: PA2573077701
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1344517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372203.1:p.Gly123Ala
CA7083184
NM_001385274.1:c.368G>C